Interaction Between Atypical Antipsychotics and the Gut Microbiome in a Bipolar Disease Cohort

被引:181
作者
Flowers, Stephanie A. [1 ]
Evans, Simon J. [2 ]
Ward, Kristen M. [1 ]
McInnis, Melvin G. [2 ]
Ellingrod, Vicki L. [1 ,2 ]
机构
[1] Univ Michigan, Coll Pharm, Rm 2060,428 Church St, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Dept Psychiat, Ann Arbor, MI 48109 USA
来源
PHARMACOTHERAPY | 2017年 / 37卷 / 03期
关键词
microbiome; atypical antipsychotics; metabolic disease; CATIE SCHIZOPHRENIA TRIAL; AKKERMANSIA-MUCINIPHILA; METABOLIC SYNDROME; WEIGHT-GAIN; OLANZAPINE; RISPERIDONE; INFLAMMATION; MECHANISMS; OBESITY; DRUGS;
D O I
10.1002/phar.1890
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
OBJECTIVES The atypical antipsychotic (AAP) class is often associated with metabolic disease, but the mechanistic underpinnings of this risk are not understood. Due to reports linking gut bacteria function to metabolic disease, we hypothesize that AAP treatment in adults results in gut dysbiosis potentiating metabolic criteria. This report describes recent findings linking AAP treatment with differences in gut microbiota communities in a human cohort with bipolar disorder (BD). METHODS In a cross-sectional design, we obtained 16S ribosomal sequences from 117 BD patients (49 AAP treated, 68 non-AAP treated). Analysis of molecular variance (AMOVA) was used to detect significant clustering of microbial communities between groups, and the inverse Simpson Diversity Index was used to calculate alpha diversity. Detection of differentially abundant operational taxonomic units (OTUs) between groups was performed using linear discriminant analysis effect size. RESULTS The AAP-treated cohort was significantly younger and had an increased body mass index compared with non-AAP-treated patients. Groups did not differ in other psychotropic medication use with the exception of higher use of benzodiazepines in the AAP cohort. We detected significant separation between microbiota communities of AAP-treated and nontreated patients (AMOVA; p=0.04). AAP-treated females showed significant decreased species diversity when compared with non-AAP-treated females (p=0.015). Males showed no significant diversity between treatment groups (p=0.8). Differentially abundant OTUs between treatment groups were OTU1, OTU25, and OTU32 that classified to Lachnospiraceae, Akkermansia, and Sutterella, respectively. CONCLUSIONS These data suggest that AAP treatment is associated with specific representation of gut bacterial families in AAP-treated patients. In addition, AAP treatment is associated with decreased species richness in female AAP-treated patients.
引用
收藏
页码:261 / 267
页数:7
相关论文
共 34 条
[1]   Age and gender effects on olanzapine and risperidone plasma concentrations in children and adolescents [J].
Aichhorn, Wolfgang ;
Marksteiner, Josef ;
Walch, Thomas ;
Zernig, Gerald ;
Hinterhuber, Hartmann ;
Stuppaeck, Christoph ;
Kemmler, Georg .
JOURNAL OF CHILD AND ADOLESCENT PSYCHOPHARMACOLOGY, 2007, 17 (05) :665-673
[2]   Host-bacterial mutualism in the human intestine [J].
Bäckhed, F ;
Ley, RE ;
Sonnenburg, JL ;
Peterson, DA ;
Gordon, JI .
SCIENCE, 2005, 307 (5717) :1915-1920
[3]   Use of the second-generation antipsychotic, risperidone, and secondary weight gain are associated with an altered gut microbiota in children [J].
Bahr, S. M. ;
Tyler, B. C. ;
Wooldridge, N. ;
Butcher, B. D. ;
Burns, T. L. ;
Teesch, L. M. ;
Oltman, C. L. ;
Azcarate-Peril, M. A. ;
Kirby, J. R. ;
Calarge, C. A. .
TRANSLATIONAL PSYCHIATRY, 2015, 5 :e652-e652
[4]   Metabolic syndrome in bipolar disorder and schizophrenia: dietary and lifestyle factors compared to the general population [J].
Bly, Michael J. ;
Taylor, Stephan F. ;
Dalack, Gregory ;
Pop-Busui, Rodica ;
Burghardt, Kyle J. ;
Evans, Simon J. ;
McInnis, Melvin I. ;
Grove, Tyler B. ;
Brook, Robert D. ;
Zoellner, Sebastian K. ;
Ellingrod, Vicki L. .
BIPOLAR DISORDERS, 2014, 16 (03) :277-288
[5]   Bariatric surgery: A systematic review and meta-analysis [J].
Buchwald, H ;
Avidor, Y ;
Braunwald, E ;
Jensen, MD ;
Pories, W ;
Fahrbach, K ;
Schoelles, K .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2004, 292 (14) :1724-1737
[6]   A Gut Feeling to Cure Diabetes: Potential Mechanisms of Diabetes Remission after Bariatric Surgery [J].
Cho, Young Min .
DIABETES & METABOLISM JOURNAL, 2014, 38 (06) :406-415
[7]  
Colton Craig W, 2006, Prev Chronic Dis, V3, pA42
[8]   Antipsychotic effects on estimated 10-year coronary heart disease risk in the CATIE schizophrenia study [J].
Daumit, Gail L. ;
Goff, Donald C. ;
Meyer, Jonathan M. ;
Davis, Vicki G. ;
Nasrallah, Henry A. ;
McEvoy, Joseph P. ;
Rosenheck, Robert ;
Davis, Sonia M. ;
Hsiao, John K. ;
Stroup, T. Scott ;
Lieberman, Jeffrey A. .
SCHIZOPHRENIA RESEARCH, 2008, 105 (1-3) :175-187
[9]   Antipsychotics and the gut microbiome: olanzapine-induced metabolic dysfunction is attenuated by antibiotic administration in the rat [J].
Davey, K. J. ;
Cotter, P. D. ;
O'Sullivan, O. ;
Crispie, F. ;
Dinan, T. G. ;
Cryan, J. F. ;
O'Mahony, S. M. .
TRANSLATIONAL PSYCHIATRY, 2013, 3 :e309-e309
[10]   Gender-dependent consequences of chronic olanzapine in the rat: effects on body weight, inflammatory, metabolic and microbiota parameters [J].
Davey, Kieran J. ;
O'Mahony, Siobhain M. ;
Schellekens, Harriet ;
O'Sullivan, Orla ;
Bienenstock, John ;
Cotter, Paul D. ;
Dinan, Timothy G. ;
Cryan, John F. .
PSYCHOPHARMACOLOGY, 2012, 221 (01) :155-169